Schinzel-Giedion syndrome with severe deafness and neurodegenerative process

Annales de Genetique

Volumn 42, Issue 4, 1999, Pages 225-230

  Alembik, Y ^a   Christmann, D ^a   De Saint Martin, A ^a   Eliot, M ^a   Dollfus, H ^a   Pauly, F ^a   Stoll, C ^a  

^a HÔPITAL DE HAUTEPIERRE   (France)

Author keywords

Alacrymia; Hearing loss; Neurodegenerative disease; Prenatal diagnosis; Schinzel Giedion syndrome

Indexed keywords

ACROCALLOSAL SYNDROME; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL MALFORMATION; EXTERNAL EAR MALFORMATION; FOLLOW UP; HEARING LOSS; HUMAN; INFANT; INNER EAR MALFORMATION; LACRIMAL APPARATUS; MALE; MENTAL DEFICIENCY; NERVE DEGENERATION; NEWBORN; PRESCHOOL CHILD;

ABNORMALITIES, MULTIPLE; BRAIN; CHILD, PRESCHOOL; COCHLEA; DEAFNESS; DISEASE PROGRESSION; EAR OSSICLES; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; NEURODEGENERATIVE DISEASES;

EID: 0033373149     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (17)